Canonical Allele Identifier: CA348391636

Gene: ERCC3

Linked Data

• MyVariant Identifiers: chr2:g.128050269C>A (hg19) ; chr2:g.127292693C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292693C>A , CM000664.2:g.127292693C>A	GRCh38
NC_000002.11:g.128050269C>A , CM000664.1:g.128050269C>A	GRCh37
NC_000002.10:g.127766739C>A	NCBI36
NG_007454.1:g.6484G>T , LRG_462:g.6484G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000285398.7:c.388G>T MANE Select	ENSP00000285398.2:p.Gly130Trp
ENST00000642308.1:c.388G>T	ENSP00000496684.1:p.Gly130Trp
ENST00000644317.1:c.246G>T	ENSP00000494012.1:p.Leu82Phe
ENST00000645233.1:c.388G>T	ENSP00000494116.1:p.Gly130Trp
ENST00000645467.1:c.388G>T	ENSP00000494889.1:p.Gly130Trp
ENST00000645736.1:c.244G>T	ENSP00000494545.1:p.Gly82Trp
ENST00000646654.1:c.388G>T	ENSP00000494526.1:p.Gly130Trp
ENST00000647169.1:c.388G>T	ENSP00000495619.1:p.Gly130Trp
ENST00000285398.6:c.388G>T	ENSP00000285398.2:p.Gly130Trp
ENST00000426778.5:c.*369G>T	ENSP00000415335.1:n.*369G>T
ENST00000445889.5:c.*431G>T	ENSP00000390888.1:n.*431G>T
ENST00000462306.5:n.302G>T
ENST00000490062.1:n.318G>T
ENST00000494464.5:n.272G>T
NM_000122.1:c.388G>T , LRG_462t1:c.388G>T	NP_000113.1:p.Gly130Trp
NM_001303416.1:c.196G>T	NP_001290345.1:p.Gly66Trp
NM_001303418.1:c.196G>T	NP_001290347.1:p.Gly66Trp
XM_011510794.1:c.388G>T	XP_011509096.1:p.Gly130Trp
XM_011510795.1:c.-69G>T	XP_011509097.1:n.-69G>T
XM_011510794.2:c.388G>T	XP_011509096.1:p.Gly130Trp
XM_017003583.1:c.-69G>T	XP_016859072.1:n.-69G>T
NM_000122.2:c.388G>T MANE Select	NP_000113.1:p.Gly130Trp
NM_001303416.2:c.196G>T	NP_001290345.1:p.Gly66Trp
NM_001303418.2:c.196G>T	NP_001290347.1:p.Gly66Trp